Zikán J, Bennett J C
Division of Clinical Immunology and Rheumatology, Department of Medicine, University of Alabama in Birmingham, University Station, Birmingham, Ala. 35294 USA.
Biochim Biophys Acta. 1973 Aug 30;317(2):447-61. doi: 10.1016/0005-2795(73)90237-7.
Human Waldenstrdm IgM (kappa) (Dau), its polypeptide chains and its F(c)5 micro and Fab micro fragments were split by cyanogen bromide (CNBr). The fragments formed by CNBr were fractionated by gel filtration, ion exchange chromatography and paper electrophoresis. They were characterized in terms of polyacrylamide disc electrophoresis, peptide maps, amino acid composition, end group determinations and limited primary structure determination. Two CNBr fragments were formed from the kappa chain, consistent with the presence of one methionine residue. Five fragments were isolated from the partially S-sulfonated micro chain. Three additional fragments were released after destruction of all disulfide bonds. The present data are unclear as to whether there are eight or nine CNBr fragments released. The comparison of CNBr pieces from the IgM, mu chain, F(c)5mu and Fab mu affords a tentative arrangement of their order, as well as the relative location of the disulfide bonds within the molecule.
人瓦尔登斯特伦巨球蛋白IgM(κ)(道氏)、其多肽链以及F(c)5μ和Fabμ片段用溴化氰(CNBr)裂解。CNBr形成的片段通过凝胶过滤、离子交换色谱法和纸电泳进行分级分离。通过聚丙烯酰胺圆盘电泳、肽图、氨基酸组成、末端基团测定和有限的一级结构测定对它们进行了表征。κ链形成了两个CNBr片段,这与存在一个甲硫氨酸残基一致。从部分S-磺化的μ链中分离出五个片段。在所有二硫键被破坏后又释放出三个片段。目前的数据尚不清楚释放出的是八个还是九个CNBr片段。对来自IgM、μ链、F(c)5μ和Fabμ的CNBr片段进行比较,初步确定了它们的顺序排列以及分子中二硫键的相对位置。